HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Ethoxybenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Ethoxybenzaldehyde | HCID 24834 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Ethoxybenzyl alcohol | HCID 80345 | — |
Reaction Steps
Mix 4-ethoxybenzaldehyde (3.3 g, 22 mmol), sodium borohydride (830 mg, 22 mmol) and absolute ethanol (25 mL). Stir at room temperature until the reaction is complete, pour onto dilute hydrochloric acid and extract into ethyl acetate. Separate the organic phase and extract the aqueous phase with ethyl acetate (2×). Combine the organic phases and dry (MgSO4). Evaporate the solvent in vacuo and purify by silica gel chromatography to give 4-ethoxybenzyl alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05248825 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-ebb9a025acde4ca7b55929f332170217 |
| Source note | uspto-grants-1993_09 |